Lataa...
Array Comparative Genomic Hybridization (aCGH) Analysis in Prader–Willi Syndrome
Prader–Willi syndrome (PWS) is due to loss of paternally expressed genes in the 15q11–q13 region generally from a paternal 15q11–q13 deletion. The proximal deletion breakpoint in the 15q11–q13 region occurs at one of two sites located within either of two large duplicons allowing for identification...
Tallennettuna:
| Julkaisussa: | Am J Med Genet A |
|---|---|
| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2008
|
| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5438264/ https://ncbi.nlm.nih.gov/pubmed/18266248 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.32249 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|